Rubus Liquid
FDA Label NDC 60986-1011

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Marco Pharma International Llc. for the product Rubus (NDC 60986-1011). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, otc - keep out of reach of children, suggested use, warnings, dosage & administration, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Rubus Fruticosus 2x

Iris Germanica 4xHPUS

Vaccinium Myrtillus 3xHPUS

Syzygium Jambolanum 3xHPUS

Okoubaka Aubrevillei 6xHPUS

The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.

Purpose

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Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Suggested Use

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Warnings

If pregnant or breast-feeding, consult a health professional before use. In case of accidental overdose, seek professional assistance or contact a poison control center immediately.

Dosage & Administration

(Read Suggested Use Section)

Inactive Ingredients

Ethyl Alcohol (52% by vol.) and Water

Package Label.Principal Display Panel


MM1

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